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OpenTrials
Completed

NCT Number: NCT06486584

Contingency Management for Problematic Behavior Reduction in the Community

This study aims to determine the feasibility and effectiveness of implementing a contingency management program in a small group of mentally ill, unhoused individuals with schizophrenia or bipolar disorder and anosognosia (a lack of insight into their mental health) in the City of Tulsa. The primary objective of the study is to decrease disruptive or problematic behaviors (e.g. interactions with police, emergency services, hospitals, shelter staff, 911 calls) by unhoused individuals in the community through monetary incentives. Up to 15 participants will meet weekly for 30 minutes with their case manager to discuss progress on life goals ($10) and for having seven days with no disruptive behaviors (or "trouble-free days") per week at each visit, they will receive an additional baseline payment of $20, increasing with continued success in subsequent weeks by $1 per week.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Laureate Institute for Brain Research

Tulsa, Oklahoma, 74136, United States

About this study

This study aims to determine the feasibility and effectiveness of implementing a contingency management program in a small group of mentally ill, unhoused individuals with schizophrenia or bipolar disorder and anosognosia (a lack of insight into their mental health) in the City of Tulsa. Tulsa's unhoused population grew nearly 7% last year to the highest numbers since the beginning of the COVID-19 pandemic according to Housing Solutions data, an organization that oversees many of the city's efforts to address homelessness. The primary objective of the study is to decrease disruptive or problematic behaviors by unhoused individuals in the community through monetary incentives.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 18-65 years old
  • Diagnosis of Schizophrenia Spectrum, Bipolar, or Related Disorders
  • Presence of Anosognosia (SUMD: Minimum combined score of 4 on questions 1) and 2); Recent (at least <6 months) history of disruptive behaviors (at least 1 disruptive behavior per week in >50% of weeks in the 6-month period prior to enrollment)
  • Receive case management services through TDC
  • Ability to comply with study procedures
  • Willingness to participate in contingency management intervention

Exclusion criteria

  • Inability to provide informed consent
  • Unstable medical conditions that would interfere with participation
  • Cognitive impairment that would interfere with participation in the study
  • History of severe aggression or violent behavior posing a risk to study staff or other participants
  • Active suicidal ideation or a history of suicide attempts within the past 12 months

Treatment and study plan

Contingency Management

Behavioral

Contingency management payment for no disruptive behaviors each week.

Primary outcomes

  1. Reduction in disruptive behaviors

    Time frame: 6 months

    Participants will decrease the frequency of disruptive behaviors in comparison with the 6-month period immediately prior to recruitment

Secondary outcomes

  1. Reduction in disruptive behaviors

    Time frame: 18 months

    Participants will decrease the frequency of disruptive behaviors in comparison with the 6-month period immediately prior to recruitment

Sponsors and collaborators

Lead sponsor

Laureate Institute for Brain Research, Inc.

Other

Collaborators

  • Tulsa Day Center

Registry information

Important dates

Study start
2023
Primary completion
2023
Study completion
2024
First posted
Jul 3, 2024
Registry last updated
Mar 4, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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